1-Butyl-4-methylpyridinium iodide

Base Information

• Chemical Name: 1-Butyl-4-methylpyridinium iodide
• CAS No.: 32353-64-3
• Molecular Formula: C10H16N.I
• Molecular Weight: 277.148
• Hs Code.: 2933399090
• European Community (EC) Number: 624-670-4
• UNII: 89A5KW6BF8
• ChEMBL ID: CHEMBL3182882
• DSSTox Substance ID: DTXSID7049267
• Mol file: 32353-64-3.mol

Synonyms:1-BUTYL-4-METHYLPYRIDINIUM IODIDE;32353-64-3;1-butyl-4-methylpyridin-1-ium;iodide;DTXSID7049267;89A5KW6BF8;SCHEMBL1502769;CHEMBL3182882;DTXCID6029123;Tox21_202689;MFCD15143656;NCGC00260237-01;1-Butyl-4-methylpyridinium iodide, 99%;CAS-32353-64-3;1-BUTYL-4-METHYLPYRIDIN-1-IUM IODIDE;Pyridinium, 1-butyl-4-methyl-, iodide (1:1)

Chemical Property of 1-Butyl-4-methylpyridinium iodide

Chemical Property:

• PSA: 3.88000
• LogP: -0.91340
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 277.03275
• Heavy Atom Count: 12
• Complexity: 93

Purity/Quality:

98% ^*data from raw suppliers

1-Butyl-4-methylpyridinium iodide 99% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): 3731243
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCC[N+]1=CC=C(C=C1)C.[I-]
• Uses: 1-Butyl-4-methylpyridinium iodide can be used:To prepare host-guest inclusion complexes of α- and β-cyclodextrins in an aqueous medium.As a halogen source in the preparation of bismuth oxyhalide semiconductors for photocatalysis applications.As a catalyst in the synthesis of allyl glycidyl carbonates by cycloaddition of epoxides with CO2.

Technology Process of 1-Butyl-4-methylpyridinium iodide

There total 1 articles about 1-Butyl-4-methylpyridinium iodide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

picoline (108-89-4) + 1-iodo-butane (542-69-8) → 1-butyl-4-methylpyridin-1-ium iodide (32353-64-3)

Guidance literature:

In ethanol; at 80 ℃;

Reference yield: 100.0%

1-butyl-4-methylpyridin-1-ium iodide (32353-64-3) + benzoic acid (65-85-0,8013-63-6) → 1-butyl-4-methylpyridinium benzoate (920759-11-1)

Guidance literature:

benzoic acid; With Amberlyst A-26 (OH^- form); In tetrahydrofuran; methanol; water; acetonitrile; at 20 ℃;

1-butyl-4-methylpyridin-1-ium iodide; In methanol;

DOI:10.3390/molecules17044007

Reference yield: 100.0%

1-butyl-4-methylpyridin-1-ium iodide (32353-64-3) → 1-butyl-4-methylpyridinium benzoate (920759-11-1)

Guidance literature:

In methanol;

DOI:10.1039/c0cc05350c

upstream raw materials:

picoline

1-iodo-butane

Downstream raw materials:

4-[(E)2-(1-n-butylpyridinium-4-yl)ethenyl] phenolate

methyl iodide

4-methyl-N-butylpyridinium tetrafluoroborate

1-butyl-4-methylpyridinium benzoate

Refernces

• 1、 Stoean, Bianca,Rugina, Dumitrita,Focsan, Monica,Craciun, Ana-Maria,Nistor, Mǎdǎlina,Lovasz, Tamas,Turza, Alexandru,Porumb, Ioan-Dan,Gál, Emese,Cristea, Castelia,Silaghi‐dumitrescu, Luminita,Astilean, Simion,Gaina, Luiza Iona. "Novel (Phenothiazinyl)vinyl‐pyridinium dyes and their potential applications as cellular staining agents". . p. 1 - 21. Retrieved 2021.
• 2、 -. "FLUORESCENT COMPOUND HAVING PROPERTY LOCALIZED IN MITOCHONDRION". Paragraph 0058-0060. . Retrieved 2017/06/29.